As events surrounding the coronavirus (COVID-19) continue to unfold, medical device companies are finding themselves facing unforeseen challenges, whether that be centralized teams now being forced to collaborate and access information remotely, clinical trials being delayed, or a myriad of other issues caused by the "new normal".
Based on data-driven insights from medical device industry professionals in the 2020 State of Medical Device Product Development & Quality Management Report, we know medical device companies’ ability to collaborate will be disrupted based on the fact that:
And yet companies that indicated that they were using best-in-class software for managing product development and quality activities are:
This in-depth webinar will cover how companies using turn-key, best-in-class QMS software are able to remain agile in order to innovate and outperform the competition.
Greenlight Guru is a modern quality management software platform used by medical device companies in over 25 countries to bring new products to market faster while simplifying regulatory compliance and reducing risk. Being the only industry specific, cloud-based eQMS, Greenlight Guru is easier to implement, easier to use and simply fits medical device processes out-of-the-box allowing companies to innovate faster and be more efficient. Visit our homepage to learn more.